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Adhesion as a Focus in Trichoderma–Root Interactions

Fungal spores, germlings, and mycelia adhere to substrates, including host tissues. The adhesive forces depend on the substrate and on the adhesins, the fungal cell surface proteins. Attachment is often a prerequisite for the invasion of the host, hence its importance. Adhesion visibly precedes colo...

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Autores principales: Taylor, James T., Harting, Rebekka, Shalaby, Samer, Kenerley, Charles M., Braus, Gerhard H., Horwitz, Benjamin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026816/
https://www.ncbi.nlm.nih.gov/pubmed/35448603
http://dx.doi.org/10.3390/jof8040372
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author Taylor, James T.
Harting, Rebekka
Shalaby, Samer
Kenerley, Charles M.
Braus, Gerhard H.
Horwitz, Benjamin A.
author_facet Taylor, James T.
Harting, Rebekka
Shalaby, Samer
Kenerley, Charles M.
Braus, Gerhard H.
Horwitz, Benjamin A.
author_sort Taylor, James T.
collection PubMed
description Fungal spores, germlings, and mycelia adhere to substrates, including host tissues. The adhesive forces depend on the substrate and on the adhesins, the fungal cell surface proteins. Attachment is often a prerequisite for the invasion of the host, hence its importance. Adhesion visibly precedes colonization of root surfaces and outer cortex layers, but little is known about the molecular details. We propose that by starting from what is already known from other fungi, including yeast and other filamentous pathogens and symbionts, the mechanism and function of Trichoderma adhesion will become accessible. There is a sequence, and perhaps functional, homology to other rhizosphere-competent Sordariomycetes. Specifically, Verticillium dahliae is a soil-borne pathogen that establishes itself in the xylem and causes destructive wilt disease. Metarhizium species are best-known as insect pathogens with biocontrol potential, but they also colonize roots. Verticillium orthologs of the yeast Flo8 transcription factor, Som1, and several other relevant genes are already under study for their roles in adhesion. Metarhizium encodes relevant adhesins. Trichoderma virens encodes homologs of Som1, as well as adhesin candidates. These genes should provide exciting leads toward the first step in the establishment of beneficial interactions with roots in the rhizosphere.
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spelling pubmed-90268162022-04-23 Adhesion as a Focus in Trichoderma–Root Interactions Taylor, James T. Harting, Rebekka Shalaby, Samer Kenerley, Charles M. Braus, Gerhard H. Horwitz, Benjamin A. J Fungi (Basel) Review Fungal spores, germlings, and mycelia adhere to substrates, including host tissues. The adhesive forces depend on the substrate and on the adhesins, the fungal cell surface proteins. Attachment is often a prerequisite for the invasion of the host, hence its importance. Adhesion visibly precedes colonization of root surfaces and outer cortex layers, but little is known about the molecular details. We propose that by starting from what is already known from other fungi, including yeast and other filamentous pathogens and symbionts, the mechanism and function of Trichoderma adhesion will become accessible. There is a sequence, and perhaps functional, homology to other rhizosphere-competent Sordariomycetes. Specifically, Verticillium dahliae is a soil-borne pathogen that establishes itself in the xylem and causes destructive wilt disease. Metarhizium species are best-known as insect pathogens with biocontrol potential, but they also colonize roots. Verticillium orthologs of the yeast Flo8 transcription factor, Som1, and several other relevant genes are already under study for their roles in adhesion. Metarhizium encodes relevant adhesins. Trichoderma virens encodes homologs of Som1, as well as adhesin candidates. These genes should provide exciting leads toward the first step in the establishment of beneficial interactions with roots in the rhizosphere. MDPI 2022-04-06 /pmc/articles/PMC9026816/ /pubmed/35448603 http://dx.doi.org/10.3390/jof8040372 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Taylor, James T.
Harting, Rebekka
Shalaby, Samer
Kenerley, Charles M.
Braus, Gerhard H.
Horwitz, Benjamin A.
Adhesion as a Focus in Trichoderma–Root Interactions
title Adhesion as a Focus in Trichoderma–Root Interactions
title_full Adhesion as a Focus in Trichoderma–Root Interactions
title_fullStr Adhesion as a Focus in Trichoderma–Root Interactions
title_full_unstemmed Adhesion as a Focus in Trichoderma–Root Interactions
title_short Adhesion as a Focus in Trichoderma–Root Interactions
title_sort adhesion as a focus in trichoderma–root interactions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026816/
https://www.ncbi.nlm.nih.gov/pubmed/35448603
http://dx.doi.org/10.3390/jof8040372
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